'1000 genomes' presentation slideshows

1000 genomes - PowerPoint PPT Presentation

UKOLN is supported by:

UKOLN is supported by:

The changing data landscape Dr Liz Lyon, Associate Director, UK Digital Curation Centre Director, UKOLN, University of Bath, UK DCC Regional Roadshow, Cardiff, December 2011. UKOLN is supported by:. This work is licensed under a Creative Commons Licence Attribution-ShareAlike 2.0.

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603 views • 60 slides
Gil McVean

Gil McVean

Gil McVean. What makes us different?. Image: Wikimedia commons. The genetic axes. Strong. Genetic disorders. Cancer. Inherited. Somatic. Complex disease. Aging. Weak. Images:Wikimedia commons. Characterising individual genomes. Image: Wikimedia commons. Image: Wikimedia commons.

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545 views • 35 slides
Association mapping: finding genetic variants for common traits & diseases

Association mapping: finding genetic variants for common traits & diseases

Association mapping: finding genetic variants for common traits & diseases. Manuel Ferreira. Genetic Epidemiology. Queensland Institute of Medical Research Brisbane. WEHI Postgraduate seminar, 31 May 2010. Why?. Understand disease aetiology.

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470 views • 33 slides
Extracting genetic variation from human genome sequences Stephen Sherry, PhD

Extracting genetic variation from human genome sequences Stephen Sherry, PhD

Extracting genetic variation from human genome sequences Stephen Sherry, PhD. pipeline for 1000 genomes cSRA deployment software to support use of NGS data post NGS analysis data sets. 1000 genomes project: goals.

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521 views • 32 slides
An introduction to the Y-chromosomal data from Phase 3 of the 1000 Genomes Project

An introduction to the Y-chromosomal data from Phase 3 of the 1000 Genomes Project

An introduction to the Y-chromosomal data from Phase 3 of the 1000 Genomes Project. Yali Xue on behalf of The 1000 Genomes Y chromosome group. Crossing over in PAR1 - 2.6Mb. Crossing over in PAR2 - 0.32Mb. Workable part of Y chromosome. Unique region ~10.4 Mb SNPs, Indels & MNPs callable.

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337 views • 14 slides
GeneGrid finding disease causing variants in NGS data

GeneGrid finding disease causing variants in NGS data

GeneGrid finding disease causing variants in NGS data. Claudia Gugenmus Genomatix Software GmbH Bayerstrasse 85a. 80335 Munich, Germany http://www.genomatix.com. Motivation. Whole genome/ exome sequencing.

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306 views • 13 slides
Laura Clarke Vertebrate Genomics laura@ebi.ac.uk

Laura Clarke Vertebrate Genomics laura@ebi.ac.uk

The 1000 Genomes project, Data Availability and Accessibility L Clarke , H Zheng Bradley, R Smith, I Streeter, E Kulesha, B. Vaughan, P. Flicek and The 1000 Genomes Project. European Bioinformatics Institute, Wellcome Trust Genome Campus, Cambridge, CB10 1SA, UK.

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156 views • 1 slides

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